Feasibility and Safety of Tethered Capsule Endomicroscopy in Patients With Barrett's Esophagus in a Multi-Center Study.


Journal

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775

Informations de publication

Date de publication:
04 2022
Historique:
received: 08 01 2021
accepted: 02 02 2021
pubmed: 8 2 2021
medline: 17 3 2022
entrez: 7 2 2021
Statut: ppublish

Résumé

Tethered capsule endomicroscopy (TCE) involves swallowing a small tethered pill that implements optical coherence tomography (OCT) imaging, procuring high resolution images of the whole esophagus. Here, we demonstrate and evaluate the feasibility and safety of TCE and a portable OCT imaging system in patients with Barrett's esophagus (BE) in a multi-center (5-site) clinical study. Untreated patients with BE as per endoscopic biopsy diagnosis were eligible to participate in the study. TCE procedures were performed in unsedated patients by either doctors or nurses. After the capsule was swallowed, the device continuously obtained 10-μm-resolution cross-sectional images as it traversed the esophagus. Following imaging, the device was withdrawn through mouth, and disinfected for subsequent reuse. BE lengths were compared to endoscopy findings when available. OCT-TCE images were compared to volumetric laser endomicroscopy (VLE) images from a patient who had undergone VLE on the same day as TCE. 147 patients with BE were enrolled across all sites. 116 swallowed the capsule (79%), 95/114 (83.3%) men and 21/33 (63.6%) women (P = .01). High-quality OCT images were obtained in 104/111 swallowers (93.7%) who completed the procedure. The average imaging duration was 5.55 ± 1.92 minutes. The mean length of esophagus imaged per patient was 21.69 ± 5.90 cm. A blinded comparison of maximum extent of BE measured by OCT-TCE and EGD showed a strong correlation (r = 0.77-0.79). OCT-TCE images were of similar quality to those obtained by OCT-VLE. The capabilities of TCE to be used across multiple sites, be administered to unsedated patients by either physicians or nurses who are not expert in OCT-TCE, and to rapidly and safely evaluate the microscopic structure of the esophagus make it an emerging tool for screening and surveillance of BE patients. Clinical trial registry website and trial number: NCT02994693 and NCT03459339.

Sections du résumé

BACKGROUND & AIMS
Tethered capsule endomicroscopy (TCE) involves swallowing a small tethered pill that implements optical coherence tomography (OCT) imaging, procuring high resolution images of the whole esophagus. Here, we demonstrate and evaluate the feasibility and safety of TCE and a portable OCT imaging system in patients with Barrett's esophagus (BE) in a multi-center (5-site) clinical study.
METHODS
Untreated patients with BE as per endoscopic biopsy diagnosis were eligible to participate in the study. TCE procedures were performed in unsedated patients by either doctors or nurses. After the capsule was swallowed, the device continuously obtained 10-μm-resolution cross-sectional images as it traversed the esophagus. Following imaging, the device was withdrawn through mouth, and disinfected for subsequent reuse. BE lengths were compared to endoscopy findings when available. OCT-TCE images were compared to volumetric laser endomicroscopy (VLE) images from a patient who had undergone VLE on the same day as TCE.
RESULTS
147 patients with BE were enrolled across all sites. 116 swallowed the capsule (79%), 95/114 (83.3%) men and 21/33 (63.6%) women (P = .01). High-quality OCT images were obtained in 104/111 swallowers (93.7%) who completed the procedure. The average imaging duration was 5.55 ± 1.92 minutes. The mean length of esophagus imaged per patient was 21.69 ± 5.90 cm. A blinded comparison of maximum extent of BE measured by OCT-TCE and EGD showed a strong correlation (r = 0.77-0.79). OCT-TCE images were of similar quality to those obtained by OCT-VLE.
CONCLUSIONS
The capabilities of TCE to be used across multiple sites, be administered to unsedated patients by either physicians or nurses who are not expert in OCT-TCE, and to rapidly and safely evaluate the microscopic structure of the esophagus make it an emerging tool for screening and surveillance of BE patients. Clinical trial registry website and trial number: NCT02994693 and NCT03459339.

Identifiants

pubmed: 33549871
pii: S1542-3565(21)00109-9
doi: 10.1016/j.cgh.2021.02.008
pmc: PMC8715859
mid: NIHMS1707174
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT03459339', 'NCT02994693']

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

756-765.e3

Subventions

Organisme : NCI NIH HHS
ID : R01 CA184102
Pays : United States

Informations de copyright

Copyright © 2022 AGA Institute. Published by Elsevier Inc. All rights reserved.

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Auteurs

Jing Dong (J)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Catriona Grant (C)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Barry Vuong (B)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Norman Nishioka (N)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Anna Huizi Gao (AH)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Matthew Beatty (M)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Grace Baldwin (G)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Aaron Baillargeon (A)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Ara Bablouzian (A)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Patricia Grahmann (P)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Nitasha Bhat (N)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Emily Ryan (E)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Amilcar Barrios (A)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Sarah Giddings (S)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Timothy Ford (T)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Emilie Beaulieu-Ouellet (E)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Seyed Hamid Hosseiny (SH)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Irene Lerman (I)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Wolfgang Trasischker (W)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Rohith Reddy (R)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Kanwarpal Singh (K)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Michalina Gora (M)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts; ICube Laboratory, CNRS, Strasbourg University, Strasbourg, France.

Daryl Hyun (D)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts.

Lucille Quénéhervé (L)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Michael Wallace (M)

Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida.

Herbert Wolfsen (H)

Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida.

Prateek Sharma (P)

Department of Gastroenterology, Kansas City Veterans Administration and University of Kansas School of Medicine, Kansas City, Missouri.

Kenneth K Wang (KK)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.

Cadman L Leggett (CL)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.

John Poneros (J)

Columbia University Irving Medical Center, New York, New York.

Julian A Abrams (JA)

Columbia University Irving Medical Center, New York, New York.

Charles Lightdale (C)

Columbia University Irving Medical Center, New York, New York.

Samantha Leeds (S)

Columbia University Irving Medical Center, New York, New York.

Mireille Rosenberg (M)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Guillermo J Tearney (GJ)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts; Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts; Harvard-MIT Division of Health Science and Technology, Cambridge, Massachusetts. Electronic address: gtearney@partners.org.

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